Leica EG1150C IFU 2v6H en 0
Leica EG1150C IFU 2v6H en 0
Leica EG1150C IFU 2v6H en 0
Leica EG1150 C
Cold Plate
The information, numerical data, notes and val- These are determined only by the contract pro-
ue judgments contained in this manual repre- visions agreed between ourselves and our cus-
sent the current state of scientific knowledge tomers.
and state-of-the-art technology as we under- Leica reserves the right to change technical
stand it following thorough investigation in this specifications as well as manufacturing pro-
field. cesses without prior notice. Only in this way is
We are under no obligation to update the pres- it possible to continuously improve the technol-
ent manual periodically and on an ongoing ogy and manufacturing techniques used in our
basis according to the latest technical devel- products.
opments, nor to provide our customers with ad- This document is protected under copyright
ditional copies, updates etc. of this manual. laws. All copyrights to this documentation are
To the extent permitted in accordance with held by Leica Biosystems Nussloch GmbH.
the national legal system as applicable in each Any reproduction of text and illustrations (or of
individual case, we shall not be held liable for any parts thereof) by means of print, photocopy,
erroneous statements, drawings, technical il- microfiche, web cam or other methods—in-
lustrations etc. contained in this manual. In cluding any electronic systems and media—
particular, no liability whatsoever is accepted requires express prior permission in writing by
for any financial loss or consequential damage Leica Biosystems Nussloch GmbH.
caused by or related to compliance with state- For the instrument serial number and year of
ments or other information in this manual. manufacture, please refer to the nameplate at
Statements, drawings, illustrations and other in- the back of the instrument.
formation regarding the contents or technical
details of the present Instructions for Use are
not to be considered warranted characteristics © Leica Biosystems Nussloch GmbH
of our products.
Leica EG1150 C 3
Table of contents
1. Important Information................................................................................................................................. 5
1.1 Symbols in the text and their meanings................................................................................................ 5
1.2 Qualification of personnel........................................................................................................................ 6
1.3 Intended use of instrument...................................................................................................................... 6
1.4 Instrument type.......................................................................................................................................... 6
2. Safety............................................................................................................................................................. 7
2.1 Safety notes............................................................................................................................................... 7
2.2 Warnings.................................................................................................................................................... 8
2.3 Integrated safety devices........................................................................................................................ 9
3. Instrument components and specifications.......................................................................................... 10
3.1 Overview – instrument parts................................................................................................................. 10
3.2 Technical Data......................................................................................................................................... 11
4. Instrument Setup..................................................................................................................................... 12
4.1 Location conditions................................................................................................................................. 12
4.2 Delivery range.......................................................................................................................................... 12
4.3 Unpacking and installation.................................................................................................................... 13
4.4 Power supply........................................................................................................................................... 15
5. Operation.................................................................................................................................................. 16
5.1 Switch on the instrument....................................................................................................................... 16
5.2 Replacing the secondary fuse.............................................................................................................. 16
5.3 Instrument malfunctions........................................................................................................................ 17
6. Cleaning and Maintenance................................................................................................................... 18
6.1 Cleaning the instrument......................................................................................................................... 18
6.2 Maintenance instructions...................................................................................................................... 18
7. Warranty and Service............................................................................................................................... 19
8. Decontamination Certificate (Master)................................................................................................ 20
Manufacturer
Leica EG1150 C 5
1. Important Information
The safety and caution notes in this chapter must be observed at all times.
Be sure to read these notes even if you are already familiar with the operation and use of other
Leica products.
These Instructions for Use must be appropriately supplemented as required by the existing reg-
ulations on accident prevention and environmental safety in the operator's country.
The protective devices located on the instrument and the accessories must not be removed or
modified. Only service personnel qualified by Leica may repair the instrument and access the
instrument's internal components.
Use only the provided power cable - this must not be replaced with a different power cable. If
the power plug does not fit in your socket, contact our service.
Residual risks
The instrument has been designed and constructed with the latest state-of-the-art technology
and according to recognized standards and regulations with regard to safety technology. Oper-
ating or handling the instrument incorrectly can place the user or other personnel at risk of in-
jury or can cause damage to the instrument or other property. The instrument may be used only
as intended and only if all of its safety features are in proper working condition. Malfunctions
that impede safety must be remedied immediately.
For current information about applicable guidelines, please refer to the CE declaration of con-
formity and on our Internet site at:
http://www.LeicaBiosystems.com
Leica EG1150 C 7
2. Safety
To prevent damage to the instrument or the specimen, only accessories authorized by Leica
may be used.
2.2 Warnings
The safety devices installed in this instrument by the manufacturer only constitute the basis
for accident prevention. Operating the instrument safely is, above all, the responsibility of the
owner, as well as the designated personnel who operate, service or clean the instrument.
To ensure trouble-free operation of the instrument, make sure to comply with the following
instructions and warnings.
• The instrument may be operated by trained laboratory personnel only. It must only be oper-
ated for the purpose of its designated use and according to the instructions contained in
these Instructions for Use.
• Safety notes on the instrument itself marked with a warning triangle indicate that the cor-
rect operating instructions (as defined in these Instructions for Use) must be followed when
operating or replacing the item marked. Nonobservance can cause accidents, injuries and/
or damage to the instrument/accessories.
• The minimum voltage (see Technical data) must be maintained while starting the refrigera-
tion unit.
The compressor needs a start-up current of approx. 25 A. A stable power supply in accor-
dance with the instrument's specifications is essential to its proper functioning. Please en-
sure that your electrical installation fulfills these preconditions prior to installing the unit.
Nonobservance causes damage to the instrument.
• Switch off the instrument each time before servicing, repairing or cleaning, and pull out the
power plug.
Leica EG115 0 C 9
3. Instrument components and specifications
Refrigeration
Illuminated system
on-off switch (inside)
(automatic fuse)
Hinged hood
(optional)
Cooling surface
Fig. 3
Leica EG115 0 C 13
4. Instrument Setup
• Connect the power cord plug (7) to the connecting port (6).
• Plug the power cord into the wall outlet.
Fig. 6
Leica EG115 0 C 15
5. Operation
5.2 Replacing the secondary fuse A miniature fuse to protect the electronic com-
ponents is located on the rear of the instrument.
Fig. 7
Leica EG115 0 C 17
6. Cleaning and Maintenance
Switch off the instrument each time before cleaning and pull out the power plug.
While handling cleaning materials, observe the safety regulations of the manufacturer and the
lab regulations valid in the country of use.
During cleaning, do not allow any liquid to penetrate inside the instrument!
To prevent scratching the surface of the instrument, do not use metallic tools with sharp edges
under any circumstances.
Work surface
• All common laboratory cleaning products suitable for the removal of paraffin (e.g. Para-
guard or xylene substitutes) can be used to clean the work area.
Only Leica service technicians are authorized to open the instrument for maintenance and re-
pair work.
Please observe the following points to ensure the instrument's reliable function over ex-
tended periods:
• Clean the instrument with care daily.
• Regularly remove dust from the ventilation slots on the back of the instrument with a
brush or vacuum cleaner.
• Have the instrument inspected at least once a year by an authorized Leica customer
service technician.
• Enter into a service contract at the end of the warranty period. For more information,
contact the relevant Leica customer service organization.
Warranty
Leica Biosystems Nussloch GmbH guarantees that the contractual prod-
uct delivered has been subjected to a comprehensive quality control
procedure based on the Leica in-house testing standards, and that the
product is faultless and complies with all technical specifications and/or
characteristics warranted.
The scope of the warranty is based on the content of the concluded
agreement. The warranty terms of your Leica sales organization or the or-
ganization from which you have purchased the contractual product shall
apply exclusively.
Service information
If you are in need of technical customer support or spare parts, please
contact your Leica representative or the Leica dealer where you pur-
chased the instrument.
Please provide the following information:
• Model name and serial number of the instrument.
• Location of the instrument and name of the person to contact.
• Reason for the service call.
• Date of delivery.
Leica EG115 0 C 19
Decontamination
8.Decontamination CertificateCertificate
(Master)
Dear Customer,
Any product that is to be returned to Leica Biosystems or serviced on site, must be cleaned and decontaminated in the appropriate manner. Since it is not possible to
decontaminate for prion diseases, such as CJD, BSE, CWD etc., equipment exposed to specimens containing prion diseases cannot be returned to Leica Biosystems
for repair. On-site repair of prion contaminated equipment will only be conducted after the Field Service Engineer has been educated in the risks, instructed in the
policies and procedures of the institution, and provided with personal protective equipment. Please fill out this confirmation carefully and enclose a copy with the
instrument. Attach the confirmation to the outside of the flight case or hand it directly to the service technician.
Packages will not be opened, nor servicing commenced until the Company or service engineer have received a satisfactory certificate. Should returned
goods be considered a hazard by the Company, they will be returned immediately to the customer at his/her expense. Note: Microtome knives must be in boxes.
Mandatory information: Fields marked with * are mandatory. Depending on whether the instrument is contaminated, please also complete either section A
or section B.
Nameplate information Model (see nameplate)* SN (see nameplate)*
Tick Box A if applicable. Otherwise please complete all parts of B, providing further
information as requested or appropriate.
A
Yes
This equipment has not been in contact with unfixed biological samples.
1 This equipment has been exposed internally or externally to hazardous materials as indicated
B Yes No
below:
Other biohazards
Chemicals/substances hazardous to health
Other hazards
Radioactivity
** Such equipment must not be returned without the written agreement of Leica Biosystems.
Yes No
3 The equipment has been prepared to ensure safe handling/transportation.
Whenever possible, please use the original transportation case/box.
Important - to avoid refusal of shipment:
Place one copy in the unit prior to packaging, or hand it over to the service engineer. Customer assumes all responsibility for the
immediate return shipment of articles sent to Leica without proper decontamination documentation.
If you have any further questions, please call your local Leica organization.
Leica Internal Use: If applicable, note corresponding Job and RAN-/RGA-Number:
Job Sheet No.: _______________ BU Return Authorization Number: ______________ SU Return Goods Authorization: ______________
Signature/Date* Institute*
.5 - 01/2013, Order-No. 14 0700 83101
Department*
Name*
20 Instructions for Use V 2.6 RevH – 07/2016
Address*
Position*
** Such equipment must not be returned without the written agreement of Leica Biosystems.
8. Decontamination Certificate (Master)
Yes No
3 The equipment has been prepared to ensure safe handling/transportation.
Whenever possible, please use the original transportation case/box.
Important - to avoid refusal of shipment:
Place one copy in the unit prior to packaging, or hand it over to the service engineer. Customer assumes all responsibility for the
immediate return shipment of articles sent to Leica without proper decontamination documentation.
If you have any further questions, please call your local Leica organization.
Leica Internal Use: If applicable, note corresponding Job and RAN-/RGA-Number:
Job Sheet No.: _______________ BU Return Authorization Number: ______________ SU Return Goods Authorization: ______________
Signature/Date* Institute*
Address*
Position*
Leica EG115 0 C 21
Notes